Zobrazeno 1 - 10
of 20
pro vyhledávání: '"C. A. Mickelson"'
Publikováno v:
Paediatr Child Health
Résumé Le trouble développemental de la coordination est une affection neurodéveloppementale qui touche de 5 % à 6 % des enfants d’âge scolaire. Il peut avoir des effets considérables sur le début du développement et le fonctionnement tout
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e43e761cc23e48c35d1c7118fa59e92
https://doi.org/10.1093/pch/pxab049
https://doi.org/10.1093/pch/pxab049
Publikováno v:
Paediatr Child Health
Developmental coordination disorder (DCD) is a neurodevelopmental condition that affects 5% to 6% of school-aged children. DCD can significantly impact early development and life-long functioning. Evidence supports promising interventions for DCD, bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc7edf8f20ee3aaf784304d761322c2e
https://europepmc.org/articles/PMC8448494/
https://europepmc.org/articles/PMC8448494/
Publikováno v:
Canadian Medical Association Journal. 187:659-665
Developmental coordination disorder is a common neuromotor condition, affecting about 5%–6% of school-aged children;[1][1] this equates to more than 400 000 Canadian children.[2][2] Despite its prevalence, developmental coordination disorder may be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8d0f1e96fff18732234a70724ad540a
https://doi.org/10.1503/cmaj.140994
https://doi.org/10.1503/cmaj.140994
Autor:
Elizabeth C. R. Mickelson, J Zwicker
BACKGROUND: The diagnosis of developmental coordination disorder (DCD) is based on four criteria outlined in the Diagnostic and Statistical Manual-5th ed. (American Psychiatric Association, 2013). One of these criteria is that the motor difficulties
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cee819c036b5351bb5bc22292aecb119
https://europepmc.org/articles/PMC5804779/
https://europepmc.org/articles/PMC5804779/
Autor:
Albert E. Chudley, Evica Rajcan-Separovic, Elizabeth C. R. Mickelson, Xudong Liu, Noémie Riendeau, Cynthia J. Forster-Gibson, Melissa Hudson, Jeanette J. A. Holden, M. Jeannette Hildebrand, M. E. Suzanne Lewis, Ying Qiao, Patrick Malenfant, Ira L. Cohen, Monica Hrynchak
Publikováno v:
Journal of Autism and Developmental Disorders. 42:1459-1469
Duplications of 7q11.23, deleted in Williams-Beuren Syndrome, have been implicated in autism spectrum disorders (ASDs). A 1.5 Mb duplication was identified in one girl with severe expressive language deficits and anxiety among 1,142 ASD individuals s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::078081f2206fc2be40f60d150be78bfe
https://doi.org/10.1007/s10803-011-1389-4
https://doi.org/10.1007/s10803-011-1389-4
Publikováno v:
The British Journal of Development Disabilities. 54:69-82
(2008). The Value of a Genetic Diagnosis for Individuals with Intellectual Disabilities: Optimising Healthcare and Function Across the Lifespan. The British Journal of Development Disabilities: Vol. 54, No. 107, pp. 69-82.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7092b9dc01f47c0d5977a680a6461149
https://doi.org/10.1179/096979508799103215
https://doi.org/10.1179/096979508799103215
Autor:
J G Hall, X Liu, E. Rajcan-Separovic, Elizabeth C. R. Mickelson, Ying Qiao, J Hildebrand, Chansonette Harvard, J. J. A. Holden, Jane Hurlburt, M. E. S. Lewis, Barbara McGillivray
Publikováno v:
Journal of Medical Genetics. 44:269-276
Background: During whole genome microarray-based comparative genomic hybridisation (array CGH) screening of subjects with idiopathic intellectual disability, we identified two unrelated individuals with a similar de novo interstitial microdeletion at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21bb948c4bc6e9f3ac1bc08ace356813
https://doi.org/10.1136/jmg.2006.045013
https://doi.org/10.1136/jmg.2006.045013
Publikováno v:
Journal of Developmental & Behavioral Pediatrics. 27:S95-S103
The Social Communication Questionnaire (SCQ) is a parent report screening measure for autism spectrum disorders (ASDs) based on the Autism Diagnostic Interview-Revised (ADI-R). To examine its validity in a young sample, the SCQ was given to parents o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29c68356134a065b0f514ed3190c986b
https://doi.org/10.1097/00004703-200604002-00007
https://doi.org/10.1097/00004703-200604002-00007
Autor:
M Koochek, M J Hildebrand, M I Van Allen, M. E. S. Lewis, E. Rajcan-Separovic, H. Wingert, Chansonette Harvard, Elizabeth C. R. Mickelson, J. J. A. Holden
Publikováno v:
Clinical Genetics. 69:124-134
Autism spectrum disorders (ASDs) are a group of neurodevelopmental disorders with a strong genetic aetiology. In approximately 1% of cases, duplication of the 15q11-13 region has been reported. We report the clinical, array-comparative genomic hybrid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::437c39cc05279e67daed98642795fe0d
https://doi.org/10.1111/j.1399-0004.2005.00560.x
https://doi.org/10.1111/j.1399-0004.2005.00560.x
Autor:
Chansonette Harvard, M Koochek, M. E. S. Lewis, S Creighton, Elizabeth C. R. Mickelson, P Malenfant, J J A Holden, Evica Rajcan-Separovic
Publikováno v:
Clinical Genetics. 67:341-351
Cri du Chat syndrome (CdCs) is a well-defined clinical entity, with an incidence of 1/15,000 to 1/50,000. The critical region for CdCs has been mapped to 5p15, with the hallmark cat-like cry sublocalized to 5p15.3 and the remaining clinical features
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9fccbbe9e5b882732d0aa8964d74204
https://doi.org/10.1111/j.1399-0004.2005.00406.x
https://doi.org/10.1111/j.1399-0004.2005.00406.x